To ask the Secretary of State for Health and Social Care, if he will estimate (a) the number of children in kinship care that receive delayed medical treatment in (i) emergencies and (ii) routine medical care resulting from the challenges in establishing a kinship carer’s parental responsibility and (b) the potential harm of such delays.
Answered on
22 May 2025
The Government does not hold the data requested. It is a legal and ethical principle that valid consent must be obtained before starting personal care, treatment, or investigations. This reflects the rights of individuals to decide what happens to their own bodies, as consent is a fundamental principle of good healthcare and professional practice. For infants and young children not competent to give or withhold consent, consent can be given by a person with parental responsibility. By law, healthcare professionals only need one person with parental responsibility to give consent for them to provide treatment. We do, however, recognise that too many babies, children, and young people are not receiving the support and care they deserve. We know that waiting times for services are far too long and we are determined to change that. The Government is committed to creating the healthiest generation of children ever, including children in care. The Government is adopting a mission-based approach and will deliver this ambition through the Health and Opportunity Missions, and through the 10-Year Plan for the National Health Service.